A film-based integrated chip for gene amplification and electrochemical detection of pathogens causing foodborne illnesses

被引:26
作者
Park, Yoo Min [1 ]
Lim, Sun Young [1 ]
Shin, Su Jeong [1 ]
Kim, Chi Hyun [1 ]
Jeong, Soon Woo [1 ]
Shin, Seol Yi [1 ]
Bae, Nam Ho [1 ]
Lee, Seok Jae [1 ]
Na, Jeongkyeong [2 ]
Jung, Gyoo Yeol [2 ]
Lee, Tae Jae [1 ]
机构
[1] Natl NanoFab Ctr NNFC, Nanobio Applicat Team, 291 Deahak Ro, Daejeon 34141, South Korea
[2] Pohang Univ Sci & Technol, Dept Chem Engn, 77 Cheongam Ro, Pohang 790784, Gyeongbuk, South Korea
基金
新加坡国家研究基金会;
关键词
Film-based polymerase chain reaction; Electrochemical DNA analysis; Point-of-care testing; POLYMERASE-CHAIN-REACTION; COMMON ELECTRONICS COMPONENTS; REAL-TIME PCR; BIOSENSING SYSTEM; DNA; SMARTPHONE; PLATFORM; DISCRIMINATION; INFECTIONS; DEVICE;
D O I
10.1016/j.aca.2018.03.061
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Given the increased interest in public hygiene due to outbreaks of food poisoning, increased emphasis has been placed on developing novel monitoring systems for point-of-care testing (POCT) to evaluate pathogens causing foodborne illnesses. Here, we demonstrate a pathogen evaluation system utilizing simple film-based microfluidics, featuring simultaneous gene amplification, solution mixing, and electrochemical detection. To minimize and integrate the various functionalities into a single chip, patterned polyimide and polyester films were mainly used on a polycarbonate housing chip, allowing simple fabrication and alignment, in contrast to conventional polymerase chain reaction, which requires a complex biosensing system at a bench-top scale. The individual integrated sensing chip could be manually fabricated in 10 min. Using the developed film-based integrated biosensing chip, the genes from the pathogens causing foodborne illnesses were simultaneously amplified based on multiple designed microfluidic chambers and Hoechst 33258, which intercalates into double-stranded DNA, to generate the electrochemical signal. The target pathogen gene was accurately analyzed by square wave voltammetry (SWV) within the 25 s, while the gel electrophoresis required about 30 min. Based on the developed integrated biosensing chip, the 1.0 x 10(1) and 1.0 x 10(2) colony-forming unit (CFU) of Staphylococcus aureus and Escherichia coli were sensitively detected with high reproducibility in the 25 s. On the basis of the significant features of the film-based molecular analysis platform, we expect that the developed sensor could be applied to the screening of various pathogens as a POCT device. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:57 / 66
页数:10
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